26172-55-4

CMIT/MIT

CMIT/MIT

别名:
CasNo.: 26172-55-4
分子式: C4H4ClNOS
分子量: 149.601
储存条件:
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中文名称: CMIT/MIT
英文名称: CMIT/MIT
CasNo.: 26172-55-4
分子式: C4H4ClNOS
分子量: 149.601

Purity 99% Min CMIT/MIT 26172-55-4 Spot Supply with Safe Transportation

  • Molecular Formula:C4H4ClNOS
  • Molecular Weight:149.601
  • Appearance/Colour:Clear to yellow liquid 
  • Vapor Pressure:0.328mmHg at 25°C 
  • Melting Point:42-45?C 
  • Refractive Index:n20/D 1.378  
  • Boiling Point:200.2 °C at 760 mmHg 
  • PKA:-4.06±0.40(Predicted) 
  • Flash Point:74.9 °C 
  • PSA:50.24000 
  • Density:1.51 g/cm3 
  • LogP:1.10020 

Isothiazolinones(Cas 26172-55-4) Usage

Safety Information

The recommended use of isothiazolinone products by the manufacturers used as wrinkle releaser is not harmful. However, allergy to skin is one of the most reported issue with isothiazolinone.

Applications

Although isothiazolinones have no direct applications, their derivatives such as 5-chloro-2-methyl-4-isothiazolin-3-on and 2-methyl-4-isothiazolin-3 which are used together as preservatives in commercial households and cosmetics products, for instance, cleaners, shampoos, and washing materials. Notably, various products that use isothiazolinones are in the market, including shampoo, hand sanitizer, and lotions. Isothiazolinones is used in these products as an inhibitor of microbial activity that could lead to the product spoiling before the expected expiration date.

Definition

ChEBI: A 1,2-thiazole that is 4-isothiazolin-3-one bearing a methyl group on the nitrogen atom and a chlorine at C-5. It is a powerful biocide and preservative and is the major active ingredient in the commercial product KathonTM.

InChI:InChI=1/C4H4ClNOS.ClH/c1-6-4(7)2-3(5)8-6;/h2H,1H3;1H

26172-55-4 Relevant articles

Preparation method of 2-methyl-4-isothiazoline-3-one aqueous solution

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Paragraph 0031-0044; 0048-0050, (2020/12/31)

The invention provides a preparation met...

Preparation method of 3-isothiazolinone compound

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Paragraph 0033-0039, (2020/12/31)

The invention discloses a preparation me...

Pipeline type continuous production method of 3-isothiazolinone compound

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Paragraph 0018, (2019/12/02)

The invention discloses a pipeline type ...

MICROBICIDE

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Paragraph 0065; 0067, (2016/12/07)

5-chloro-2-methyl-4-isothiazolin-3-yn as...

26172-55-4 Process route

N,N'-dimethyl-3,3'-dithiodipropionamide
999-72-4

N,N'-dimethyl-3,3'-dithiodipropionamide

5-chloro-2-methyl-2H-isothiazol-3-one
26172-55-4

5-chloro-2-methyl-2H-isothiazol-3-one

Conditions
Conditions Yield
With chlorine; potassium iodide; In ethyl acetate; at 40 - 55 ℃; for 0.25h;
95%
With sulfuryl dichloride; In 1,2-dichloro-ethane;
 
N,N'-dimethyl-3,3'-dithiodipropionamide; With chlorine; In water; ethyl acetate;
With hydrogenchloride; magnesium(II) nitrate hexahydrate; magnesium oxide; In water; ethyl acetate; toluene; at 40 - 80 ℃; for 3h; pH=1 - 4; Solvent;
 
N,N'-dimethyl-3,3'-dithiodipropionamide
999-72-4

N,N'-dimethyl-3,3'-dithiodipropionamide

5-chloro-2-methyl-2H-isothiazol-3-one
26172-55-4

5-chloro-2-methyl-2H-isothiazol-3-one

2-methyl-3-isothiazolone
2682-20-4

2-methyl-3-isothiazolone

Conditions
Conditions Yield
With thionyl chloride; In 1,2-dichloro-ethane; at 10 ℃; for 2h;
56%
18%
With chlorine; In ethyl acetate; acetonitrile; at 5 - 10 ℃; for 1h; Solvent; Temperature; Overall yield = 85 percent;
 

26172-55-4 Upstream products

  • 999-72-4
    999-72-4

    N,N'-dimethyl-3,3'-dithiodipropionamide

  • 1003-07-2
    1003-07-2

    3-oxo-2,3-dihydroisothiazole

  • 107-06-2
    107-06-2

    1,2-dichloro-ethane

  • 52334-99-3
    52334-99-3

    N-methyl-3-mercaptopropionamide

26172-55-4 Downstream products

  • 26530-20-1
    26530-20-1

    2-octyl-isothiazol-3-one

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